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BIO SB, INC.

United States·US-MF-000036462

Last updated September 17, 2026

What BIO SB, INC. makes

Bio SB, Inc. manufactures in vitro diagnostic (IVD) products for immunohistochemistry, including chromogenic substrates, enzyme-linked detection kits, and antibody-based reagents. Their portfolio includes enzyme immunohistochemistry substrates like DAB and AEC, as well as specific detection antibodies such as cytokeratin and CD cell markers. Control slides and reagents for analytes like Helicobacter pylori, Candida albicans, and BAP1 are also produced, alongside specialized digestion solutions for tissue processing.

The company’s products are classified under FDA’s Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for laboratory use in diagnostic testing and are regulated under U.S. FDA guidelines. The manufacturer operates within the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Bio SB, Inc. manufacture?

Bio SB, Inc. specializes in in vitro diagnostic (IVD) products primarily used in immunohistochemistry (IHC) testing. Their portfolio includes chromogenic substrates like DAB (brown) and AEC (red) for enzyme-linked detection, antibody-based reagents for detecting specific analytes (such as cytokeratin and CD cell markers), and control slides for validation purposes. Examples include reagents for Helicobacter pylori, Candida albicans, and specialized tissue digestion solutions like the Mohs ImmunoDigestor. These products are designed for laboratory use in diagnostic workflows.

Where is Bio SB, Inc. based, and how does that affect its regulatory standing?

Bio SB, Inc. is based in the United States. Since it manufactures devices regulated by the FDA, its products must comply with U.S. regulatory requirements. The company’s devices fall under FDA’s Class I classification, which generally involves lower-risk devices requiring less stringent premarket review. However, compliance with FDA guidelines—such as listing in the UDI database—remains essential for market authorization.

Which regulatory registries or databases list Bio SB, Inc.’s devices?

Bio SB, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized way for the FDA to track and identify medical devices in the U.S. market. Listing in this database ensures traceability and compliance with FDA requirements for Class I devices, though it does not imply individual device approval—only that the manufacturer has registered their products as required.

How are Bio SB, Inc.’s devices classified by regulatory authorities?

Bio SB, Inc.’s devices are classified under the FDA’s Class I category. This classification is based on risk assessment: Class I devices are generally considered low-risk and pose minimal potential harm to users. As a result, they typically require less regulatory oversight than higher-risk classes (e.g., Class II or III), though they must still meet FDA compliance standards, such as proper labeling, manufacturing controls, and UDI registration. Classification does not guarantee market authorization—only that the device falls under a specific regulatory pathway.

What is the primary purpose of Bio SB, Inc.’s in vitro diagnostic (IVD) products?

Bio SB, Inc.’s IVD products are designed for laboratory use in immunohistochemistry (IHC) and related diagnostic testing. These include chromogenic substrates (e.g., DAB for brown staining), antibody reagents for detecting specific proteins (like cytokeratin or CD markers), and control slides to validate test accuracy. For example, their Helicobacter pylori control slides or BAP1 antibodies help pathologists confirm the presence of specific biomarkers in tissue samples. The products support accurate diagnostic workflows in clinical or research settings.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
5385 , Hollister Avenue, Santa Barbara, CA, United States
Website
biosb.com
LinkedIn
—
Facebook
—
Phone
+1(800)561-1145
PRRC Contact
Jessica Dunston
EUDAMED SRN
US-MF-000036462
FDA FEI Number
3008773547
DUNS Number
102855447

Catalogue (5547)

Page 103 of 111
DeviceModel / ReferenceRegistriesClassStatus
Cytokeratin LMW CAM5.2, CAM5.2, MMab BSB 2060
EUDAMEDFDA UDI
IVD GeneralActive
Tinto TIA-1, RBT-TIA1, RMab BSB-3782-7
EUDAMEDFDA UDI
IVD GeneralActive
CD68, KP-1, MMab BSB 2715
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GFAP, RM246, RMab BSB-3766-7
EUDAMEDFDA UDI
IVD GeneralActive
pTau Phospho|Thr 181, BSB-176, MMab BSB-3807-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Brachyury, RBT-TBXT, RMab BSB 3491
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Androgen Receptor, BSB-4, MMab BSB 6071
EUDAMEDFDA UDI
IVD GeneralActive
Cadherin17|LI-Cadherin, EP86, RMab BSB 6852
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CEA, BSB-13, MMab BSB 5339
EUDAMEDFDA UDI
IVD GeneralActive
NKX3.1, EP356, RMab BSB 3118
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PD-L1|CD274, 28-8, RMab BSB-2371-15
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CD34, QBEnd|10, MMab BSB 3681
EUDAMEDFDA UDI
IVD GeneralActive
CEACAM7, BSB-168, MMab BSB-3791-01
EUDAMEDFDA UDI
IVD GeneralActive
Herpes Simplex Virus I, 10A3, MMab BSB 2688
EUDAMEDFDA UDI
IVD GeneralActive
CD21, EP64, RMab BSB 5202
EUDAMEDFDA UDI
IVD GeneralActive
Tinto SOX-10, BSB-62, MMab BSB 2209
EUDAMEDFDA UDI
IVD GeneralActive
Thyroid Peroxidase, EP159, RMab BSB 2618
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IgE|FITC, Polyclonal, GPab BSB-3011-7
EUDAMEDFDA UDI
IVD GeneralActive
TLE1, BSB-142, MMab BSB-3784-1
EUDAMEDFDA UDI
IVD GeneralActive
CD1a, EP80, RMab BSB 5139
EUDAMEDFDA UDI
IVD GeneralActive
MTAP, RBT-MTAP, RMab BSB-3739-05
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD103|ITGAE, EP206, RMab BSB 2861
EUDAMEDFDA UDI
IVD GeneralActive
CD117, RM359, RMab BSB-3758-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MLH1, G168-728, MMab BSB 5765
EUDAMEDFDA UDI
IVD GeneralActive
Tinto GLUT1, EP141, RMab BSB 6781
EUDAMEDFDA UDI
IVD GeneralActive
MUC1, RBT-MUC1, RMab BSB-3788-01
EUDAMEDFDA UDI
IVD GeneralActive
Osteonectin|SPARC, BSB-93, MMab BSB 3263
EUDAMEDFDA UDI
IVD GeneralActive
Tinto MUC-4, EP256, RMab BSB 2552
EUDAMEDFDA UDI
IVD GeneralActive
MSH2, BSB-147, MMab BSB-3722-01
EUDAMEDFDA UDI
IVD GeneralActive
Tinto ICOS|CD278, RM417, RMab BSB-3731-15
EUDAMEDFDA UDI
IVD GeneralActive
Cyclin D1, RBT-14, RMab BSB 5369
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Estrogen Receptor, BSB-1, MMab BSB 2740
EUDAMEDFDA UDI
IVD GeneralActive
TintoFast CK 5 and 6, D5 and 16B4, MMab BSB 3666
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Collagen Type IV, RBT-COL4, RMab BSB-3777-15
EUDAMEDFDA UDI
IVD GeneralActive
Maspin, BSB-92, MMab BSB 3268
EUDAMEDFDA UDI
IVD GeneralActive
ICOS|CD278, RM417, RMab BSB-3731-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD45RO, UCHL-1, MMab BSB 5261
EUDAMEDFDA UDI
IVD GeneralActive
PDGFR-B, RBT-PDGFRB, RMab BSB 2354
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PSMA, EP192, RMab BSB 6345
EUDAMEDFDA UDI
IVD GeneralActive
ZFAND3, BSB-169, MMab BSB-3797-1
EUDAMEDFDA UDI
IVD GeneralActive
Tinto EGFR Phospho, EP11, RMab BSB 6716
EUDAMEDFDA UDI
IVD GeneralActive
Factor XIIIa, EP292, RMab BSB 5509
EUDAMEDFDA UDI
IVD GeneralActive
STAR, EP226, RMab BSB 3633
EUDAMEDFDA UDI
IVD GeneralActive
PGP 9.5, BSB-46, MMab BSB 2115
EUDAMEDFDA UDI
IVD GeneralActive
Tinto PMS2, EP51, RMab BSB 2119
EUDAMEDFDA UDI
IVD GeneralActive
Tinto CD35, RLB25, MMab BSB 5232
EUDAMEDFDA UDI
IVD GeneralActive
Tinto IMP-3|1GF2BP3, EP286, RMab BSB 2966
EUDAMEDFDA UDI
IVD GeneralActive
CD42b, EP409, RMab BSB 3507
EUDAMEDFDA UDI
IVD GeneralActive
Tinto FOXP1, EP137, RMab BSB 6753
EUDAMEDFDA UDI
IVD GeneralActive
Tinto Cytokeratin LMW CAM5.2, CAM5.2, MMab BSB 2056
EUDAMEDFDA UDI
IVD GeneralActive

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